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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources October 9, 2024
Displaying entries 69176 - 69200 of 71927 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID Gene Symbol FlyGlycoDB Evidence Code Names ▼ References
DOID:2921 glomerulonephritis HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:22241891
DOID:326 ischemia RGD:621861 Rattus norvegicus (Norway rat) 89805 Angpt2
  • PMID:19672036
DOID:65 connective tissue disease HGNC:11158 Homo sapiens (human) 6632 SNRPD1
  • PMID:2477448
DOID:3908 lung non-small cell carcinoma HGNC:10473 Homo sapiens (human) 864 RUNX3
  • PMID:18349282
DOID:14250 Down syndrome HGNC:11132 Homo sapiens (human) 6616 SNAP25
  • PMID:12499044
DOID:10591 pre-eclampsia HGNC:11917 Homo sapiens (human) 7133 TNFRSF1B
  • PMID:21505354
DOID:5603 T-cell acute lymphoblastic leukemia HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:13141 uveitis HGNC:11766 Homo sapiens (human) 7040 TGFB1
  • PMID:9008650
DOID:1936 atherosclerosis HGNC:9206 Homo sapiens (human) 5446 PON3
  • PMID:20182519
DOID:3525 middle cerebral artery infarction HGNC:7997 Homo sapiens (human) 3084 NRG1
  • PMID:20691195
  • PMID:30206770
DOID:9119 acute myeloid leukemia HGNC:2438 Homo sapiens (human) 1440 CSF3
  • PMID:10673519
DOID:2988 antiphospholipid syndrome HGNC:9451 Homo sapiens (human) 5624 PROC
  • PMID:25196808
DOID:10763 hypertension RGD:3810 Rattus norvegicus (Norway rat) 24808 Tacr3
  • PMID:2471579
DOID:9279 hyperhomocysteinemia RGD:1359175 Rattus norvegicus (Norway rat) 306761 F12
  • PMID:16046705
DOID:0080630 B-lymphoblastic leukemia/lymphoma HGNC:386 Homo sapiens (human) 8644 AKR1C3
  • PMID:26116659
DOID:9119 acute myeloid leukemia HGNC:5991 Homo sapiens (human) 3552 IL1A
  • PMID:2460157
DOID:65 connective tissue disease HGNC:11155 Homo sapiens (human) 6629 SNRPB2
  • PMID:2968364
DOID:11054 urinary bladder cancer HGNC:6001 Homo sapiens (human) 3558 IL2
  • PMID:3262172
DOID:219 colon cancer HGNC:5195 Homo sapiens (human) 9956 HS3ST2
  • PMID:12527896
DOID:178 vascular disease HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:22081301
DOID:224 transient cerebral ischemia RGD:3184 Rattus norvegicus (Norway rat) 24598 Nos1
  • PMID:23806217
DOID:5199 ureteral obstruction HGNC:6000 Homo sapiens (human) 3557 IL1RN
  • PMID:21975862
DOID:8805 intermediate coronary syndrome HGNC:775 Homo sapiens (human) 462 SERPINC1
  • PMID:8122184
DOID:0060074 ductal carcinoma in situ HGNC:8591 Homo sapiens (human) 5062 PAK2
  • PMID:22886747
DOID:11984 hypertrophic cardiomyopathy HGNC:2422 Homo sapiens (human) 1431 CS
  • PMID:10354207

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Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024